FDA 510(k)

Irrisept 抗菌伤口冲洗

K号: K240552 · 2024-06-18

决定日期2024-06-18

产品代码FRO

决定实质等同

器械摘要

Irrisept Antimicrobial Wound Lavage is the device name listed in this FDA 510(k) record. The listed applicant is Irrimax Corporation. It received FDA 510(k) clearance on 2024-06-18 under 510(k) number K240552. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

常见问题

What is the Irrisept Antimicrobial Wound Lavage?

Irrisept Antimicrobial Wound Lavage is a medical device that received FDA 510(k) clearance on 2024-06-18. The listed applicant is Irrimax Corporation. The 510(k) number is K240552.

When did Irrisept Antimicrobial Wound Lavage receive FDA 510(k) clearance?

Irrisept Antimicrobial Wound Lavage received FDA 510(k) clearance on 2024-06-18, under 510(k) number K240552.

Who is the listed applicant for Irrisept Antimicrobial Wound Lavage?

The FDA 510(k) record lists Irrimax Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Irrisept Antimicrobial Wound Lavage?

The FDA product code for Irrisept Antimicrobial Wound Lavage is FRO. This falls under the Anesthesiology category.

列明Irrimax Corporation为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K222804Irrisept 抗菌伤口冲洗 K210536Irrisept 抗菌伤口冲洗 K202222Irrisept 创面清创和清洗系统

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